GB607124A - Process for the manufacture of crystallized glucose of very high purity - Google Patents

Process for the manufacture of crystallized glucose of very high purity

Info

Publication number
GB607124A
GB607124A GB11480/45A GB1148045A GB607124A GB 607124 A GB607124 A GB 607124A GB 11480/45 A GB11480/45 A GB 11480/45A GB 1148045 A GB1148045 A GB 1148045A GB 607124 A GB607124 A GB 607124A
Authority
GB
United Kingdom
Prior art keywords
crystallizer
per cent
crystals
purity
heated
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB11480/45A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
GLUCOSERIES REUNIES STE AME
Original Assignee
GLUCOSERIES REUNIES STE AME
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by GLUCOSERIES REUNIES STE AME filed Critical GLUCOSERIES REUNIES STE AME
Publication of GB607124A publication Critical patent/GB607124A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C13SUGAR INDUSTRY
    • C13KSACCHARIDES OBTAINED FROM NATURAL SOURCES OR BY HYDROLYSIS OF NATURALLY OCCURRING DISACCHARIDES, OLIGOSACCHARIDES OR POLYSACCHARIDES
    • C13K1/00Glucose; Glucose-containing syrups
    • C13K1/10Crystallisation

Landscapes

  • Chemical & Material Sciences (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Emergency Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biochemistry (AREA)
  • Organic Chemistry (AREA)
  • Saccharide Compounds (AREA)

Abstract

In a continuous process for crystallizing glucose monohydrate only a fraction of the partially crystallized mass is withdrawn from the crystallizer, and is replaced by an equal volume of solution to be crystallized, preferably by a solution of purity not greater than 86 per cent, the process being characterised by the mass in the crystallizer being kept permanently between 20 DEG and 30 DEG C. The added solution, preferably heated above 80 DEG C., melts small and irregular crystals and the large crystals, after one washing approach 100 per cent purity. The crystal size may be increased by withdrawing a portion of one mass from one crystallizer, heating to 70 DEG C. and returning it to the crystallizer. Crystals of different types may be obtained in one cycle by adding more solution to the crystallizer than that withdrawn for centrifuging, (which yields a small quantity of crystals of very high purity), and feeding a second crystallizer with an amount equal to the excess added to the first, to yield a larger quantity of crystals which are smaller, but still capable of being centrifuged. In examples: (1) a solution of 86 per cent reducing sugars is concentrated to 40 DEG C. Boum<\>ae, under vacuum at 70 DEG C. in an evaporator, is further heated to 75 DEG C. and passed to a crystallizer kept at 25 DEG C. About 10 per cent of the volume in the crystallizer is drawn-off daily to a centrifuge and replaced immediately by fresh juice at 75 DEG C., from the evaporator. The crystals are dried, sifted and bagged, and the mother liquor is mixed with a glucose syrup, concentrated, and casked or made into slabs; (2) 80 per cent of the juice introduced daily to the crystallizer is cooled to 40 per cent before introduction, the remainder being heated to 85 DEG C. The third of the quantity added is centrifuged after crystallization to yield crystals of 100 per cent purity, and the other two thirds are passed to a second crystallizer from which an equal quantity is passed each day to a centrifuge to yield crystals of 99.5 per cent purity. The mother liquors are treated as in (1). (3) glucose juice of 86 per cent purity is heated to 80 DEG C. and fed to a crystallizer maintained at 25-30 DEG C. A quantity equal to one-third of the daily feed is withdrawn from the crystallizer and centrifuged to give crystals of 100 per cent purity, a quantity equal to the remaining two-thirds of the daily feed being passed to, and divided between, two other crystallizers from which an equal amount is withdrawn and centrifuged to give crystals of 99.6 per cent purity. The mother liquors from the first centrifuge are heated to 60 DEG C. and introduced into the second two crystallizers (the amount withdrawn for centrifuging being correspondingly increased) while the mother liquors from the second centrifuge are mixed with syrup or molasses and casked to give an eating syrup. To obtain a mass of large crystals in the crystallizer in starting the process, 10 per cent of the cooled mass is daily drawn-off, heated to 80-90 per cent and returned immediately to the crystallizer. Juice of 90-92 per cent purity may be used for the crystallization process to give a higher crystal yield, but the mother liquors have then not such a good taste as when juice of a lower purity is used.
GB11480/45A 1944-04-29 1945-05-05 Process for the manufacture of crystallized glucose of very high purity Expired GB607124A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
BE607124X 1944-04-29

Publications (1)

Publication Number Publication Date
GB607124A true GB607124A (en) 1948-08-26

Family

ID=3875116

Family Applications (1)

Application Number Title Priority Date Filing Date
GB11480/45A Expired GB607124A (en) 1944-04-29 1945-05-05 Process for the manufacture of crystallized glucose of very high purity

Country Status (4)

Country Link
BE (1) BE455554A (en)
FR (1) FR910473A (en)
GB (1) GB607124A (en)
NL (1) NL61429C (en)

Also Published As

Publication number Publication date
NL61429C (en)
BE455554A (en)
FR910473A (en) 1946-06-07

Similar Documents

Publication Publication Date Title
JPH0553480B2 (en)
US2588449A (en) Levulose dihydrate
US4357172A (en) Process for continuous crystallization of alpha monohydrate dextrose utilizing high agitation
GB607124A (en) Process for the manufacture of crystallized glucose of very high purity
US2032160A (en) Sugar manufacturing process
US2069064A (en) Syrup
US2175369A (en) Manufacture of dextrose
US1640717A (en) Manufacture of large-grained dextrose
US1521830A (en) Manufacture of dextrose
US1571212A (en) Method of making grape sugar
US2102380A (en) Process of crystallizing pure d-glucono-delta-lactone
US1471347A (en) Method of making grape sugar
US1985255A (en) Process for the preparation of crystalline gluconic acid
US2501914A (en) Recovery of sucrose from molasses
US2150146A (en) Manufacture of dextrose
RU2158311C1 (en) Sugar production process
US1693118A (en) High-purity crystalline dextrose
US3547696A (en) Isothermal crystallization of dextrose
US1890913A (en) Manufacture of hydrous dextrose from high purity solutions
SU1406170A1 (en) Method of crystallizing fructose
US1750939A (en) Method of making dextrose
US2150197A (en) Manufacture of dextrose
US2430855A (en) Purification of tartaric acid
US3207782A (en) Process for crystallization of alkali metal glutamates
US1862511A (en) Process for the preparation of d-glucono-ò-lactone